#chronic joint problems
Explore tagged Tumblr posts
Text
I did somethingggggg idk what in the last 45 minutes that fucked up my finger I don't know what I didddddddddd
(my best guess is I fucking subluxated the fucking thing but I don't typically have that happen especially not on my left hand, usually my shoulders, ribs, hips, knees, and toes get all fucked like this but I guess I get to enjoy the every time I shift even a little bit so does my hand
#chronic joint problems#well. usual issue adjacent? maybe?#subluxation#probably#i'm just not used to it happening to my fingers#everywhere else is pretty typical#hopefully i won't have to consider an urgent care i'd really really rather not need one bc that's a lot of money (usa health care....)#at least it doesn't feel broken? been there done that no thanks#admittedly#i am bitching/whining a bit#how-fucking-ever#fuck my bones bc they keep doing this shit more and more frequently :)
1 note
·
View note
Text
"You're always so chipper and excited even though you're in pain, I could never."
Bethany, if I wasn't chipper and excited about the most mundane things like bees and dice, then I would literally be bedrotting all day every day, sobbing because my entire life is falling apart because I have no answers or relief to pain that doctors think is fake. So I will take joy in my trinkets and rollerskating while my body allows because one day I won't be able to.
#chronic illness#disabled#chronic disability#chronically ill#chronic disease#other chronic illness bs#chronicpain#disablity#undiagnosed chronic illness#disability#chronic pain#chronic fatigue#nerve pain#joint pain#back pain#disabilities#actually disabled#invisible disability#physically disabled#cpunk#angry cripple#cripple life#cripple problems#cripple punk#cripplepunk#crip punk#spooniestrong#spoonie#spoonie life#low spoons
2K notes
·
View notes
Text
So sad about the United Health CEO :( has he tried yoga?
#/s#chronically ill#chronic pain#chronic illness#chronic fatigue#chronic inflammation#actually disabled#disabled#disability#disabilties#endometriosis#ehlers danlos syndrome#joint hypermobility#hypermobile ehlers danlos#hypermobile eds#psoriatic arthritis#chronic illness memes#potsie#pots#pots syndrome#fibromyalgia#pcos#polycystic ovarian syndrome#arthritis#type one diabetic#type 1 diabetes#diabetes#type one diabetes#type 1 diabetic#chronic illness problems
768 notes
·
View notes
Text
they should invent walking that doesn't make you feel like you're going to keel over and die
#disability#disabled#physically disabled#me/cfs#myalgic encephalomyelitis#joint pain#joint problems#cripple punk#physical disability#mobility aid#cane user#mobility aid user#ow my joints#chronic fatigue#chronic pain#chronic illness#chronically ill#chronic migraine#long covid
5K notes
·
View notes
Text
Weather: *changes*
My joints: We're just going to die.
#shitpost#spoonie#cripple punk#arthritis#chronic pain warrior#joint problems#joint pain#it's funny because it's true
644 notes
·
View notes
Text


I was in so much pain here, but my outfit was so cute! 💜
#problem project#disabled girl#disabled#disabled community#chronic pain#disability#chronic illness#chronic fatigue#actually disabled#current cane user#cane user#girl who uses a cane#disabled and cute#chronic joint pain#joint pain
162 notes
·
View notes
Text
Happy First of May!!
Hello! May is EDS (Ehlers Danlos Syndrome) awareness month! As a person with suspected EDS and with chronic symptoms, this is a very important topic to me. EDS is hard to diagnose, and many patients fly under the radar of healthcare professionals which can cause them to suffer lack of treatment and forces them to live with their painful symptoms.
More Information about EDS and associated variations has been attached below and the infographs were originally found on an instagram account that I follow at the username the_chronic_chronicles






#hypermobile ehlers danlos#ehlers danlos syndrome#ehlers danlos zebra#ehlers danlos problems#ehlers danlos awareness#ehlers danlos life#heds#hypermobility#hypermobile eds#hypermobile joints#hypermobile problems#Vascular EDS#veds#chronic joint pain#chronic illness#chronic pain#chronically ill#chronic illness awareness
532 notes
·
View notes
Text
It's the little things that hurts.
The way people don't get you can't do the things they do, at least without costing you so much.
The way the doors of shops or buildings used to fly open at the slightest touch and now they seems to weight a hundred tons.
The way my mother in law asked me if I wanted orange juice and when I said yes she put two oranges and a old manual juicer. I was too ashamed to admit how much it would cost me to do it this way. So I did it, fighting the tears and then couldn't use my arm for a week.
The way I can't get out of my apartment sometimes because even if there is a lift, there's also stairs between my apartment door and the lift and between the lift and the building door. Why make a lift at all if it's not even accessible because of the stairs? (I can't move out. I have neither the money nor the spoons.)
The way the new building the local bookshop moved into makes things so much harder for me than the old one. There was so much unused stairs that I could sit and rest for as long as I needed. Now in the new building the stairs are so narrow you can't think of sitting on them, you'll just block the way. And there's no chair or bench anywhere in this 4 stories building. You just can't sit and rest there.
The way the city is getting rid of public benches and putting in their stead blocks of concrete with metal spikes on them to dissuade homeless people to sleep on them, which is wrong on its own, but also impacts disabled people. There's less and less places where to sit and rest during a walk through the city.
It's people laughing when I can't open a bottle of soda.
It's people gossiping behind my back, saying "oh they are a junky" because I takes so many meds, including the ones for the pain, but not only for that.
It's me being too ashamed to be disabled at a relatively young age and having an invisible disability. It's me being too ashamed to ask for accommodations. It's me being too ashamed to ask for a seat in the bus when all of them are already taken. It's the society making me ashamed of myself.
It's life itself, mocking me, and the world joining in the good laugh at my expense.
#physical disability#disability problems#disability#disabilties#disabled#actually disabled#actually physically disabled#actually chronically ill#chronically ill#chronic illness#chronic pain#chronic fatigue#rheumatism#ankylosing spondylitis#joint pain#ehlers danlos syndrome#rheumatoid arthritis#rheumarthritis#accomodation#disability awareness#disability aids#arthritis
500 notes
·
View notes
Text
my joints after the slightest physical exertion be like:
ouch ouchie ouch ouch ouchie ouch ouch ouch ouchie ouch ouch ouch ouchie ouch ouch
#joint pain#chronically fatigued#chronic illness#chronic pain#spoonie#flare up#pain flare up#chronic illness things#undiagnosed chronic illness#chronic fatigue#disabled#spoonie problems
170 notes
·
View notes
Text
Every winter I want to find whoever invented the electric heating pad and dip them down low and kiss them so sweetly
#weeks of on and off winter storms is diabolical#my joints are full of so much hatred im shocked it hasnt crystallized#fibro#fibromyalgia#fibro flare#fibro problems#hypermobility#hypermobility syndrome#joint pain#chronic pain#chronic illness#chronic fatigue#disabled#disability
140 notes
·
View notes
Text
I've received my HeDS diagnosis
After 23 years of struggling and medical gaslighting, my condition and struggle is finally recognised and I'll be able to get everything I need. I'm so happy I could cry
#hypermobile ehlers danlos#ehlers danlos syndrome#hypermobile eds#heds#chronically ill#hypermobile joints#hypermobility#chronic pain#chronic disability#spoonie#disabled#actually disabled#hypermobile problems#celebration#diagnosis
69 notes
·
View notes
Text
hurts to walk on four legs
hurts to walk on two legs
hurts to sit for too long
hurts to stand still
hurts to move
fuck.
#chronic pain#chronic illness#joint pain#chronic joint pain#fibropain#fibromyalgia#hypermobility#hypermobile spectrum disorder#chronic fatigue#chronically ill#chronic issues#ow ow ouch#chronically ill teen#fibro problems#my school moved the fire drill meeting place from the front on the school (accessible) to the football field (not) and wtf??#helpppp#therianthropy#therian#dog therian#dogkin#dog posting#german shepherd therian#alterhuman#otherkin#poetry?#im so tired
114 notes
·
View notes
Text
SAY IT WITH ME: MEDICAL GASLIGHTING IS MALPRACTICE
#chronic illness#disabled#chronic disability#chronically ill#chronic disease#other chronic illness bs#disablity#undiagnosed chronic illness#chronic pain#chronic fatigue#nerve pain#joint pain#disabilities#disability#actually disabled#disability rights#disability advocacy#invisible disability#physically disabled#doctors suck#medical stuff#medical gaslighting#medical malpractice#cripple life#cripple problems#cripple punk#angry cripple#cripplepunk
3K notes
·
View notes
Text
I wanna work out and get stronger, it would help with some of my disability symptoms. The ironic bit is that if my condition is what doctors think it is that means I'll struggle to build muscle. And even barring that, my fatigue and my pain make it difficult to walk around campus let alone go home and work out.
My physically abled gymbro friend told me to just do a little every day, and I know he means well but I don't have the energy to get dressed or brush my teeth most days.
#disabled#physically disabled#physical disability#disabilties#disability#working out#joint problems#joint pain#chronically ill#chronic illness#chronic pain#chronic fatigue#cripple posting#cripple punk#angry cripple#queer cripple#crip punk
61 notes
·
View notes
Text
"You were fine as a child/teen"-Was I though?
I've been told countless times that it's unfathomable, that it doesn't make sense, that I am chronically ill now, because I was "healthy" growing up, I was "active" and "normal."
"you were fine" they say
Frustratingly, they are wrong. I was not "fine" and I masked my symptoms heavily. In a lot of cases I didn't know that what I was going through was abnormal.
I remember the many times a year (every month/every other month) I was ill with cold & flu, tonsillitis, chickenpox, rashes, broken bones, sprains, stomach problems, pain and exhaustion.
I remember the 2 years in my teens where I had chronic knee and leg pain that was blamed on growing pains. It affected me so much my attendance in school dropped to 62% & irritated my mum so much that I failed to continue finding medical care for it and "carried on" as if I was fine.
Growing up, being ill was a burden, almost not allowed. If you were ill, you were an annoyance, a nuisance, forced to get on with it. It irritated the people around you, if you were ill with a n y t h i n g in my childhood home.
I remember throughout my whole childhood that at least one week out of the month, I'd get so exhausted I would come home from school and go straight to sleep until shouted down for dinner and I'd go back to bed.
Many times I remember coming home from school and college absolutely depleted of everything and faceplanting on my bed for 2 to 3 hours.
I remember how much I wanted to be involved in some activities but didn't have the energy and was accused of being lazy, anti social or ungrateful of opportunities.
I remember being hospitalised with chronic stomach pains, they suspected appendicitis, but when they could find nothing I was released home with nothing further done for another 15 years. I was accused of attention seeking or just wanting to skip out school.
I remember being unable to tell anybody how I felt whether it was physical or mental. When I did reach out I was told I'm too soft, I'm being dramatic, I'm just making it all up. When I did say "I'm in pain" I was told its not that bad, I'm not dying and that I "won't get any sympathy" from them.
When I went to University & got freshers flu, I was bed-bound for 9 weeks but told it was depression.
Eventually, I couldn't carry on from all the above. Now I'm bed-bound/housebound for life.
Please, tell me again, that I was "fine"
#chronic life#chronic pain#chronically ill#chronic illness#chronic fatigue#spoonie problems#fibromyalgia#myalgic encephalomyelitis#pots#ptsd#joint pain#chronic disability#chronic fatigue syndrome
491 notes
·
View notes
Text
"It's the most wonderful time of the year" oh fuck y'all it's cold and my joints are killing me!
#shitpost#disabled problems#spoonie#cold months#winter#cripple punk#chronic pain warrior#arthritis#joint pain
141 notes
·
View notes